# K031312: Rta Model D Retinal Thickness Analyzer

- Pathway: 510(k) (Special)
- Applicant: Talia Technology, Ltd.
- Decided: May 6, 2003 after 12 days
- Product code: HLI (Ophthalmoscope, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.1570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K000731 (2000). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K000731: Modification to Rta Retinal Thickness Analyzer, Talia Technology, Ltd. (2000)

## Indications for use
The RTA Model D Retinal Thickness Analyzer (“RTA”) is a computerized slitlamp biomicroscope that is intended to provide manual and computerized tomography of the retina in vivo. The RTA scans successive slit images on the fundus, without the need for a contact lens, to determine the thickness and the inner structure of the retin,a, both by observation of the slit images and by computer analysis of these images. It is indicated for assessing the area and location of retinal thickness abnormalities, such as thickening due to macular edema and atrophy associated with degenerative diseases, and for visualizing other retinal pathologies.

Source page: https://510kreport.com/device/K031312
Methodology: https://510kreport.com/methodology
